Oromandibular-limb hypogenesis syndrome

MONDO:0017139

Oromandibular-limb hypogenesis syndromes (OLHS) are a group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) characterized by the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandible (hypoglossia, aglossia, micrognathia, glossopalatine ankylosis, cleft palate, and gingival anomalies).

Also known as: Oroacral syndrome, oro-mandibular-limb hypogenesis syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with Oromandibular-limb hypogenesis syndrome itself.

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↑ Hereditary disease (18206) ↑ Oromandibular-limb anomalies syndrome (0)

Sub-types of Oromandibular-limb hypogenesis syndrome

Charlie M syndrome 0 trials
Hypoglossia-hypodactyly syndrome 0 trials
Glossopalatine ankylosis 0 trials
Isolated congenital hypoglossia/aglossia 0 trials
2 sub-types
- Isolated congenital aglossia 0 trials
- Isolated congenital hypoglossia 0 trials

Including sub-types (0) Tagged with Oromandibular-limb hypogenesis syndrome (0)

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